United States · Bill · HR
H.R. 13103 (94th)
A bill to amend the Federal Food, Drug, and Cosmetic Act to require that the identity of the manufacturer of a prescription drug appear on the label of the package from which the drug is to be dispensed.
Introduced
7 April 1976
Last action
—
Status
Referred to House Committee on Interstate and Foreign Commerce.
Sponsors
—
Subjects
Discovery layer
Source updated
1 August 2024
Summary
Requires, under the Federal Food, Drug, and Cosmetic Act, that the identity of the manufacturer of a prescription drug must appear on the label of the package from which the drug is to be dispensed.
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Votes
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Versions
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Documents
1 official file
Introduced in House
summary · EN · 7 April 1976
Sponsors
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Related records
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Sources
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- Official source: https://www.congress.gov/bill/94th-congress/house-bill/13103
- Open data entity: https://api.congress.gov/v3/bill/94/hr/13103